EP0906404A2 - Thickening agent for aqueous hydrogen peroxide solutions - Google Patents

Thickening agent for aqueous hydrogen peroxide solutions

Info

Publication number
EP0906404A2
EP0906404A2 EP97927126A EP97927126A EP0906404A2 EP 0906404 A2 EP0906404 A2 EP 0906404A2 EP 97927126 A EP97927126 A EP 97927126A EP 97927126 A EP97927126 A EP 97927126A EP 0906404 A2 EP0906404 A2 EP 0906404A2
Authority
EP
European Patent Office
Prior art keywords
weight
hydrogen peroxide
alkyl
alcohol
aqueous hydrogen
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP97927126A
Other languages
German (de)
French (fr)
Other versions
EP0906404B1 (en
Inventor
Nuria Bonastre
Rafael Pi Subirana
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF Personal Care and Nutrition GmbH
Original Assignee
Henkel AG and Co KGaA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP0906404A2 publication Critical patent/EP0906404A2/en
Application granted granted Critical
Publication of EP0906404B1 publication Critical patent/EP0906404B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3947Liquid compositions
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N59/00Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/65Mixtures of anionic with cationic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/86Mixtures of anionic, cationic, and non-ionic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/34Derivatives of acids of phosphorus
    • C11D1/345Phosphates or phosphites
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/523Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • the application relates to thickeners for aqueous hydrogen peroxide solutions, containing fatty acid alkanolamides, alkyl ether sulfates and, if appropriate, alkyl ether phosphates and / or alkyl polyglycol ethers and the use of the mixtures as thickeners for aqueous hydrogen peroxide solutions.
  • a number of bleaching and cleaning agents are known from the prior art, but they primarily have a higher viscosity.
  • DE-OS 15 67 570 German Offenlegungsschrift DE-OS 15 67 570 (Henkel)
  • liquid or pasty concentrates containing active oxygen are known, which are obtained by reacting phosphorus pentoxide with low molecular weight alcohols and hydrogen peroxide.
  • DE-A1 42 02 720 German patent application DE-A1 42 02 720 (Henkel) formulations for simultaneous desizing, boiling and bleaching of cellulose-containing textile materials are lien known that contain anionic surfactants, ethoxylated fatty alcohols and hydrogen peroxide.
  • the agents are unsuitable for cleaning hard surfaces.
  • viscous bleaching agents can be prepared by adding fatty alcohol polyglycol ethers and ethoxylated phosphoric acid esters to hydrogen peroxide solutions.
  • the object of the invention was then to provide new additives for aqueous bleaching agents based on hydrogen peroxide, with the aid of which the disadvantages described can be reliably overcome
  • the invention relates to thickeners for aqueous hydrogen peroxide solutions containing - based on the active substance content of the agents -
  • the agents give aqueous bleaches based on hydrogen peroxide a sufficiently high and stable viscosity and thereby enable the incorporation of perfumes without clouding.
  • the surfactant component proves to be stable against active oxygen compounds and reliably prevents redeposition of dirt particles once they have been dissolved.
  • R 1 CO represents an aliphatic, saturated or unsaturated acyl radical having 6 to 22 carbon atoms
  • R 2 represents hydrogen or an optionally hydroxyl-substituted alkyl radical having 1 to 4 carbon atoms and n represents numbers from 2 to 4.
  • the Alkanoiamide, acidic for example, condensation products of caproic acid, caprylic acid, 2-ethylhexanoic acid, Cap ⁇ nklare, Launnklare, Isotridecansaure, myristic acid, palmitic acid, Palmolemsaure, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, Linoiensaure, Elaeosteannsaure, arachic acid, gadoleic, ßehensaure and Represent erucic acid and its technical mixtures with mono- or diethanoiamine.
  • coconut or stearic acid fatty acid aikanolamides are preferably used.
  • ether sulfates which form component (b) are known anionic surfactants which are produced on an industrial scale by SO 3 - or chlorosulfonic acid (CSA) sulfation of alkyl polyglycol ethers and subsequent neutralization.
  • CSA chlorosulfonic acid
  • ether sulfates are suitable which follow the formula (II)
  • R 3 for a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms, n for numbers from 1 to 10 and X for an alkali and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium stands.
  • Typical examples are the sulfates of addition products with an average of 1 to 10 and in particular 2 to 5 moles of ethylene oxide with capron alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, oleyl alcohol, isostyl alcohol, isostyl alcohol hol, petroselmyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and brassidyl alcohol and their technical mixtures, in the form of their sodium and / or magnesium salts.
  • the ether sulfates can be either a conventional or a restricted homolog distribution exhibit. It is particularly preferred to use ether sulfates based on adducts of on average 2 to 3 mol ethylene oxide with technical C12 / 14 or C12 / 18 coconut oil alcohol fractions in the form of their sodium and / or magnesium salts.
  • Alkyl ether phosphates which form component (c) are also known anionic surfactants which are usually prepared by reacting ethoxylated fatty alcohols with phosphorus pentoxide. Depending on the use ratio of the components, technical mixtures are obtained which predominantly contain mono- and dialkyl esters, in addition to triesters, phosphoric acid and unreacted alcohol. Overviews on this topic are available from R.S. Cooper and G.lmokawa in J.Am.Oil.Chem.Soc. 41, 337 (1964) and 55, 839 (1978), H.Distler in Tenside Detergents 12, 263 (1975) and O'Lennick in Soap, Cosm.Chem.Spec. 7, 26 (1986).
  • the alkyl ether phosphates preferably follow the formula (III)
  • R 4 is a linear or branched alkyl radical having 6 to 12 carbon atoms
  • R 5 is a group R 4 (OCH2CH2) P or X
  • p is a number from 1 to 5
  • X is hydrogen, an alkali and / or alkaline earth metal .
  • Typical examples of ethoxylated phosphoric acid esters which are considered as component (c) in the sense of the invention are mono- and / or dialkyl esters based on adducts of 1 to 10, preferably 2 to 8, moles of ethylene oxide with capronalcohol, caprylic alcohol , 2-ethylhexyl alcohol, capric alcohol and / or lauryl alcohol.
  • the degree of esterification can be 1 to 2.5 and preferably 1.3 to 2.1. Particular preference is given to ethoxylated phosphoric acid esters of the formula (III) in which R 4 is a 2-ethylhexyl radical, R 5 is X, p is a number from 1 to 3 and X is hydrogen.
  • R 4 is a 2-ethylhexyl radical
  • R 5 is X
  • p is a number from 1 to 3
  • X is hydrogen.
  • alkyl ether phosphates is particularly advantageous for the production of opacifying agents.
  • the thickeners can contain, as optional component (d), alkyl polyglycol ethers of the formula (IV)
  • R 6 represents an alkyl and / or alkenyl radical having 6 to 22 carbon atoms and q represents numbers from 1 to 10.
  • suitable nonionic surfactants of the formula (IV) are addition products of average 1 to 10 and in particular 5 to 8 moles of ethylene oxide with 1 mole of capron alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol and cetyl alcohol , Palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, linolyl alcohol, linolenyl alcohol, elaeostearyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and brassidyl alcohol and their technical mixtures.
  • Addition products of 5 to 8 moles of ethylene oxide with fatty alcohols having 12 to 18 and in particular 16 to 18 carbon atoms are preferably used, which can have a conventional, but preferably a narrow, homolog distribution.
  • component (d) is of particular advantage with regard to the incorporation of perfumes and the peroxide stability.
  • the agents according to the invention impart a sufficiently high and stable viscosity to aqueous bleaching agents based on peroxide.
  • the agents are preferably in the form of aqueous preparations which have a non-aqueous content of 10 to 50 and preferably 20 to 40% by weight.
  • Another object of the invention relates to their use as thickeners for aqueous hydrogen peroxide solutions.
  • the aqueous hydrogen peroxide solutions are preferably aqueous bleaches on the market which accordingly generally have an active substance content of 1 to 10 and preferably 5 to 8% by weight.
  • the agents are usually used in amounts of 1 to 5 and preferably 2 to 4% by weight, based on their non-aqueous content and the aqueous hydrogen peroxide solutions.
  • the aqueous hydrogen peroxide solutions may contain, as auxiliaries and additives, further peroxide-stable surfactants or hydrotropes, such as, for example, alkyl sulfates, alkyl sulfonates, alkylbenzenesulfonates, xylene sulfonates, sarcosinates, taurides, isethionates, sulfosuccinates, ether carboxylic acids, betaines, sugar esters, amine oxides and alkyl oligoglyides.
  • the sum of these additional surfactants preferably makes up at most 10% by weight of the total amount of surfactants in the formulation.
  • the agents can contain peroxide-stable fragrances, optical brighteners, dyes and pigments in a total amount of 0.01 to 0.5% by weight, based on the agents.
  • the fragrances known as peroxide-resistant include, for example, monocyclic and bicyclic monoterpene alcohols and their esters with acetic or propionic acid (for example isobomeal, dihydroterpene oil, isobornyl acetate, dihydroterpenyl acetate).
  • the optical brighteners can be, for example, the potassium salt of 4,4'-bis (1,2,3-triazolyl) - (2 -) - stilbin-2,2-sulfonic acid, which is sold under the brand name Phorwite® BHC 766 is distributed.
  • Possible color pigments include green chlorophthalocyanines (Pigmosol® Green, Hostaphine® Green) or yellow Solar Yellow BG 300 (Sandoz).
  • the agents according to the invention are produced by stirring. If necessary, the product obtained can be decanted or filtered to remove foreign bodies and / or agglomerates.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Detergent Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Cosmetics (AREA)

Abstract

The proposal is for novel thickening agents for aqueous hydrogen peroxide solutions, containing, in relation to the active substance content of the agent, (a) 10 to 90 wt % fatty acid alkanolamides, (b) 5 to 20 wt % alkyl ether sulphates, (c) 0 to 5 wt % alkyl ether phosphates and (d) 0 to 60 wt % alkyl polyglycol ether, with the proviso that the weights add up to 100 wt %. The agents ensure a reliable and permanent viscosity setting and make the inclusion of perfumes easier without the risk of turbidity. 00000

Description

Verdickungsmittel für wäßrige Wasserstoffperoxidlösungen Thickener for aqueous hydrogen peroxide solutions
Gebiet der ErfindungField of the Invention
Gegenstand der Anmeldung sind Verdickungsmittel für wäßrige Wasserstoffperoxidlösungen, enthal¬ tend Fettsäurealkanolamide, Alkylethersulfate sowie gegebenenfalls Alkyletherphosphate und/oder Alkylpolyglycolether und die Verwendung der Mischungen als Verdickungsmittel für wäßrige Wasser- stoffperoxidlösungen.The application relates to thickeners for aqueous hydrogen peroxide solutions, containing fatty acid alkanolamides, alkyl ether sulfates and, if appropriate, alkyl ether phosphates and / or alkyl polyglycol ethers and the use of the mixtures as thickeners for aqueous hydrogen peroxide solutions.
Stand der TechnikState of the art
In der Vergangenheit haben sich in den Bereichen Hygiene und Desinfektion solche Bleichmittel auf der Grundlage von Wasserstoffperoxid bewährt, die über eine bemerkenswerte Viskosität verfügen und sich daher sowohl für die Behandlung horizontaler als auch geneigter und vor allem vertikaler Ober¬ flächen eignen. Die Viskosität dieser Mittel bewirkt, daß die Kontaktzeit zwischen diesen und den zu behandelnden Oberflächen wesentlich größer ist als bei handelsüblichen Flüssigprodukten, die rasch von der Oberfläche abfließen. Daneben besteht jedoch auch ein Bedürfnis nach niedrigviskosen, in ihrer Konsistenz wasserähnlichen Produkten, die rasch und vollständig von den behandelnden Flächen ablaufen.In the past, such bleaching agents based on hydrogen peroxide have proven themselves in the areas of hygiene and disinfection, which have a remarkable viscosity and are therefore suitable for the treatment of horizontal as well as inclined and, above all, vertical surfaces. The viscosity of these agents has the effect that the contact time between them and the surfaces to be treated is considerably longer than in the case of commercially available liquid products which flow off rapidly from the surface. In addition, however, there is also a need for low-viscosity, water-like consistency products that run off quickly and completely from the treatment surfaces.
Aus dem Stand der Technik sind eine Reihe von Bleich- und Reinigungsmitteln bekannt, die jedoch vor¬ nehmlich eine höhere Viskosität aufweisen. Aus der Deutschen Offenlegungsschrift DE-OS 15 67 570 (Henkel) sind beispielsweise flüssige oder pastenförmige, Aktivsauerstoff enthaltende Konzentrate be¬ kannt, die man durch Umsetzung von Phosporpentoxid mit niedermolekularen Alkoholen und Wasser¬ stoffperoxid erhält. Aus der Deutschen Patentanmeldung DE-A1 42 02 720 (Henkel) sind Formu¬ lierungen zum gleichzeitigen Entschlichten, Abkochen und Bleichen von cellulosehaltigen Textilmateria- lien bekannt, die anionische Tenside, ethoxylierte Fettalkohole und Wasserstoffperoxid enthalten. Die Mittel sind jedoch für die Reinigung harter Oberflächen ungeeignet Gemäß der Deutschen Offenle- gungsschrift DE-A1 44 18 847 (Henkel) lassen sich viskose Bleichmittel durch Zugabe von Fettalkohol- polyglycolethern und ethoxylierten Phosphorsäureestern zu Wasserstoffperoxidlösungen herstellen.A number of bleaching and cleaning agents are known from the prior art, but they primarily have a higher viscosity. From German Offenlegungsschrift DE-OS 15 67 570 (Henkel), for example, liquid or pasty concentrates containing active oxygen are known, which are obtained by reacting phosphorus pentoxide with low molecular weight alcohols and hydrogen peroxide. From the German patent application DE-A1 42 02 720 (Henkel) formulations for simultaneous desizing, boiling and bleaching of cellulose-containing textile materials are lien known that contain anionic surfactants, ethoxylated fatty alcohols and hydrogen peroxide. However, the agents are unsuitable for cleaning hard surfaces. According to German Offenlegungsschrift DE-A1 44 18 847 (Henkel), viscous bleaching agents can be prepared by adding fatty alcohol polyglycol ethers and ethoxylated phosphoric acid esters to hydrogen peroxide solutions.
Trotz des umfangreichen Stands der Technik, der an dieser Stelle nur exemplarisch wiedergegeben werden kann, sind die Produkte des Marktes im Hinblick auf ihr Leistungsvermögen nach wie vor nicht völlig zufriedenstellend: Die Viskosität ist häufig zu hoch und verändert sich im Laufe der Lagerung, die Tensidkomponente ist gegenüber Aktivsauerstoff nicht ausreichend stabil, gelöster Schmutz wird wie¬ der auf der Oberfläche redeponiert und läßt diese stumpf erscheinen, schließlich lassen sich Parfüm¬ stoffe nicht ohne die Gefahr von unerwünschten Austrübungen einarbeitenDespite the extensive state of the art, which can only be reproduced here as an example, the products on the market are still not completely satisfactory in terms of their performance: The viscosity is often too high and changes during storage, the surfactant component is not sufficiently stable to active oxygen, loosened dirt is repositioned on the surface and makes it appear dull, after all perfumes cannot be incorporated without the risk of undesirable clouding
Die Aufgabe der Erfindung hat somit dann bestanden, neue Zusatzstoffe für wäßrige Bleichmittel auf Basis von Wasserstoffperoxid zur Verfügung zu stellen, mit deren Hilfe die geschilderten Nachteile zu¬ verlässig überwunden werden könnenThe object of the invention was then to provide new additives for aqueous bleaching agents based on hydrogen peroxide, with the aid of which the disadvantages described can be reliably overcome
Beschreibung der ErfindungDescription of the invention
Gegenstand der Erfindung sind Verdickungsmittel für wäßrige Wasserstoffperoxidlosungen, enthaltend - bezogen auf den Aktivsubstanzgehalt der Mittel -The invention relates to thickeners for aqueous hydrogen peroxide solutions containing - based on the active substance content of the agents -
(a) 10 bis 90, vorzugsweise 40 bis 80 Gew -% Fettsäurealkanolamide,(a) 10 to 90, preferably 40 to 80% by weight of fatty acid alkanolamides,
(b) 5 bis 20, vorzugsweise 8 bis 16 Gew.-% Alkylethersulfate,(b) 5 to 20, preferably 8 to 16% by weight of alkyl ether sulfates,
(c) 0 bis 5, vorzugsweise 1 bis 4 Gew.-% Alkyletherphosphate und(c) 0 to 5, preferably 1 to 4% by weight of alkyl ether phosphates and
(d) 0 bis 60, vorzugsweise 4 bis 50 Gew -% Alkyipolyg lycolether(d) 0 to 60, preferably 4 to 50% by weight alkyl polyglycol ether
mit der Maßgabe, daß sich die Gewichtsangaben zu 100 Gew -% erganzenwith the proviso that the weight details add up to 100% by weight
Überraschenderweise wurde gefunden, daß die Mittel wäßrigen Bleichmittel auf Wasserstoff¬ peroxidbasis eine ausreichend hohe und stabile Viskosität verleihen und dabei die Einarbeitung von Parfümstoffen ermöglichen, ohne daß es zu Austrübungen kommt. Die Tensidkomponente erweist sich gegenüber Aktivsauerstoffverbindungen stabil und verhindert die Wiederablagerung einmal gelöster Schmutzteilchen zuverlässig. FettsäurealkanolamideSurprisingly, it has been found that the agents give aqueous bleaches based on hydrogen peroxide a sufficiently high and stable viscosity and thereby enable the incorporation of perfumes without clouding. The surfactant component proves to be stable against active oxygen compounds and reliably prevents redeposition of dirt particles once they have been dissolved. Fatty acid alkanolamides
Fettsäurealkanolamide, die die Komponente (a) bilden, folgen der Formel (I),Fatty acid alkanolamides which form component (a) follow the formula (I),
R2 R 2
I R1CON(CH2)nOH (I)IR 1 CON (CH 2 ) nOH (I)
in der R1CO für einen aliphatischen, gesättigten oder ungesättigten Acylrest mit 6 bis 22 Kohlen¬ stoffatomen, R2 für Wasserstoff oder einen gegebenenfalls hydroxysubstituierten Alkylrest mit 1 bis 4 Kohlenstoffatomen und n für Zahlen von 2 bis 4 steht. Die Alkanoiamide können beispielsweise Kondensationsprodukte von Capronsaure, Caprylsäure, 2-Ethylhexansaure, Capπnsäure, Launnsäure, Isotridecansaure, Myristinsaure, Palmitinsaure, Palmolemsaure, Stearinsäure, Isostearinsäure, Ölsaure, Elaidinsaure, Petroselinsaure, Linolsaure, Linoiensaure, Elaeosteannsaure, Arachinsaure, Gadolein- saure, ßehensaure und Erucasäure sowie deren technische Mischungen mit Mono- oder Diethanoiamin darstellen Vorzugsweise werden Kokos- oder Steaπnsäurefettsäureaikanolamide eingesetzt.in which R 1 CO represents an aliphatic, saturated or unsaturated acyl radical having 6 to 22 carbon atoms, R 2 represents hydrogen or an optionally hydroxyl-substituted alkyl radical having 1 to 4 carbon atoms and n represents numbers from 2 to 4. The Alkanoiamide, acidic, for example, condensation products of caproic acid, caprylic acid, 2-ethylhexanoic acid, Capπnsäure, Launnsäure, Isotridecansaure, myristic acid, palmitic acid, Palmolemsaure, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, Linoiensaure, Elaeosteannsaure, arachic acid, gadoleic, ßehensaure and Represent erucic acid and its technical mixtures with mono- or diethanoiamine. Coconut or stearic acid fatty acid aikanolamides are preferably used.
AlkylethersulfateAlkyl ether sulfates
Alkylethersulfate ("Ethersulfate"), die die Komponente (b) bilden, stellen bekannte anionische Tenside dar, die großtechnisch durch S03- oder Chlorsulfonsaure (CSA)-Sulfatierung von Alkylpolyglycolethern und nachfolgende Neutralisation hergestellt werden. Im Sinne der Erfindung kommen Ethersulfate in Betracht, die der Formel (II) folgen,Alkyl ether sulfates ("ether sulfates"), which form component (b), are known anionic surfactants which are produced on an industrial scale by SO 3 - or chlorosulfonic acid (CSA) sulfation of alkyl polyglycol ethers and subsequent neutralization. For the purposes of the invention, ether sulfates are suitable which follow the formula (II)
R30-(CH2CH2θ)mS03X (II)R30- (CH 2 CH2θ) mS0 3 X (II)
in der R3 für einen linearen oder verzweigten Alkyl- und/oder Alkenylrest mit 6 bis 22 Kohlenstoff¬ atomen, n für Zahlen von 1 bis 10 und X für ein Alkali- und/oder Erdalkalimetall, Ammonium, Alkyl- ammonium, Alkanolammonium oder Glucammonium steht. Typische Beispiele sind die Sulfate von Anlagerungsprodukten von durchschnittlich 1 bis 10 und insbesondere 2 bis 5 Mol Ethylenoxid an Capronalkohol, Caprylalkohol, 2-Ethylhexylalkohol, Caprinalkohol, Laurylalkohol, Isotridecylalkohol, My- ristylalkohol, Cetylalkohol, Palmoleylalkohol, Stearylalkohol, Isostearylalkohol, Oleylalkohol, Elaidylalko- hol, Petroselmylalkohol, Arachylalkohol, Gadoleylalkohol, Behenylalkohol, Erucylalkohol und Brassidyl- alkohol sowie deren technische Mischungen, in Form ihrer Natrium- und/oder Magnesiumsalze Die Ethersulfate können dabei sowohl eine konventionelle als auch eine eingeengte Homologenverteilung aufweisen. Besonders bevorzugt ist der Einsatz von Ethersulfaten auf Basis von Addukten von durch¬ schnittlich 2 bis 3 Mol Ethylenoxid an technische C12/14- bzw. C12/18- Kokosfettalkoholfraktionen in Form ihrer Natrium- und/oder Magnesiumsalze.in R 3 for a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms, n for numbers from 1 to 10 and X for an alkali and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium stands. Typical examples are the sulfates of addition products with an average of 1 to 10 and in particular 2 to 5 moles of ethylene oxide with capron alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, oleyl alcohol, isostyl alcohol, isostyl alcohol hol, petroselmyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and brassidyl alcohol and their technical mixtures, in the form of their sodium and / or magnesium salts. The ether sulfates can be either a conventional or a restricted homolog distribution exhibit. It is particularly preferred to use ether sulfates based on adducts of on average 2 to 3 mol ethylene oxide with technical C12 / 14 or C12 / 18 coconut oil alcohol fractions in the form of their sodium and / or magnesium salts.
AlkyletherphosphateAlkyl ether phosphates
Alkyletherphosphate, die die Komponente (c) bilden, stellen ebenfalls bekannte anionische Tenside dar, die üblicherweise durch Umsetzung von ethoxylierten Fettalkoholen mit Phosphorpentoxid herge¬ stellt werden. In Abhängigkeit des Einsatzverhältnisses der Komponenten werden dabei technische Ge¬ mische erhalten, die überwiegend Mono- und Dialkylester, neben Triestem, Phosphorsäure und nicht umgesetzten Alkohol enthalten. Übersichten zu diesem Thema sind beispielsweise von R.S. Cooper sowie G.lmokawa in J.Am.Oil.Chem.Soc. 41, 337 (1964) bzw. 55, 839 (1978), H.Distler in Tenside Detergents 12, 263 (1975) und O'Lennick in Soap, Cosm.Chem.Spec. 7, 26 (1986) erschienen. Vorzugsweise folgen die Alkyletherphosphate der Formel (III),Alkyl ether phosphates which form component (c) are also known anionic surfactants which are usually prepared by reacting ethoxylated fatty alcohols with phosphorus pentoxide. Depending on the use ratio of the components, technical mixtures are obtained which predominantly contain mono- and dialkyl esters, in addition to triesters, phosphoric acid and unreacted alcohol. Overviews on this topic are available from R.S. Cooper and G.lmokawa in J.Am.Oil.Chem.Soc. 41, 337 (1964) and 55, 839 (1978), H.Distler in Tenside Detergents 12, 263 (1975) and O'Lennick in Soap, Cosm.Chem.Spec. 7, 26 (1986). The alkyl ether phosphates preferably follow the formula (III)
OXOX
I R4(OCH2CH2)pO-P-OR5 (III)IR 4 (OCH 2 CH 2 ) pO-P-OR5 (III)
II 0II 0
in der R4 für einen linearen oder verzweigten Alkylrest mit 6 bis 12 Kohlenstoffatomen, R5 für eine Gruppe R4(OCH2CH2)P oder X, p für Zahlen von 1 bis 5 und X für Wasserstoff, ein Alkali- und/oder Erdalkalimetall steht. Typische Beispiele für ethoxylierte Phosphorsäureester, die im Sinne der Erfin¬ dung als Komponente (c) in Betracht kommen, sind Mono- und/oder Dialkylester auf Basis von Adduk¬ ten von 1 bis 10, vorzugsweise 2 bis 8 Mol Ethylenoxid an Capronalkohol, Caprylalkohol, 2-Ethylhexyl- alkohol, Caprinalkohol und/ oder Laurylalkohol. Der Veresterungsgrad kann dabei 1 bis 2,5 und vor¬ zugsweise 1 ,3 bis 2,1 betragen. Besonders bevorzugt sind ethoxylierte Phosphorsäureester der Formel (III), in der R4 für einen 2-Ethylhexylrest, R5 für X, p für Zahlen von 1 bis 3 und X für Wasserstoff steht. Die Mitverwendung von Alkyletherphosphaten ist für die Herstellung von trübungsfreien Mitteln beson¬ ders vorteilhaft. Alkylpolyqlvcoletherin which R 4 is a linear or branched alkyl radical having 6 to 12 carbon atoms, R 5 is a group R 4 (OCH2CH2) P or X, p is a number from 1 to 5 and X is hydrogen, an alkali and / or alkaline earth metal . Typical examples of ethoxylated phosphoric acid esters which are considered as component (c) in the sense of the invention are mono- and / or dialkyl esters based on adducts of 1 to 10, preferably 2 to 8, moles of ethylene oxide with capronalcohol, caprylic alcohol , 2-ethylhexyl alcohol, capric alcohol and / or lauryl alcohol. The degree of esterification can be 1 to 2.5 and preferably 1.3 to 2.1. Particular preference is given to ethoxylated phosphoric acid esters of the formula (III) in which R 4 is a 2-ethylhexyl radical, R 5 is X, p is a number from 1 to 3 and X is hydrogen. The use of alkyl ether phosphates is particularly advantageous for the production of opacifying agents. Alkyl polyglycol ether
Schließlich können die Verdickungsmittel als fakultative Komponente (d) Alkylpolyglycolether der For¬ mel (IV) enthalten,Finally, the thickeners can contain, as optional component (d), alkyl polyglycol ethers of the formula (IV)
R<O(CH2CH20)qH (IV)R <O (CH 2 CH 2 0) q H (IV)
in der R6 für einen Alkyl- und/oder Alkenylrest mit 6 bis 22 Kohlenstoffatomen und q für Zahlen von 1 bis 10 steht. Typische Beispiele für geeignete nichtionische Tenside der Formel (IV) sind Anlagerungs¬ produkte von durchschnittliche 1 bis 10 und insbesondere 5 bis 8 Mol Ethylenoxid an jeweils 1 Mol Capronalkohol, Caprylalkohol, 2-Ethylhexylalkohol, Caprinalkohol, Laurylalkohol, Isotridecylalkohol, My- ristylalkohol, Cetylalkohol, Palmoleylalkohol, Stearylalkohol, Isostearylalkohol, Oleylalkohol, Elaidylalko- hol, Petroselinylalkohol, Linolylalkohol, Linolenylalkohol, Elaeostearylalkohol, Arachylalkohol, Gadoleyl- alkohol, Behenylalkohol, Erucylalkohol und Brassidylalkohol sowie deren technische Mischungen. Vorzugsweise werden Anlagerungsprodukte von 5 bis 8 Mol Ethylenoxid an Fettalkohole mit 12 bis 18 und insbesondere 16 bis 18 Kohlenstoffatomen eingesetzt, die eine konventionelle, vorzugsweise jedoch eine eingeengte Homologenverteilung aufweisen können. Die Mitverwendung der Komponente (d) ist im Hinblick auf die Einarbeitung von Parfümstoffen und die Peroxidstabilität von besonderem Vorteil.in which R 6 represents an alkyl and / or alkenyl radical having 6 to 22 carbon atoms and q represents numbers from 1 to 10. Typical examples of suitable nonionic surfactants of the formula (IV) are addition products of average 1 to 10 and in particular 5 to 8 moles of ethylene oxide with 1 mole of capron alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol and cetyl alcohol , Palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, linolyl alcohol, linolenyl alcohol, elaeostearyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and brassidyl alcohol and their technical mixtures. Addition products of 5 to 8 moles of ethylene oxide with fatty alcohols having 12 to 18 and in particular 16 to 18 carbon atoms are preferably used, which can have a conventional, but preferably a narrow, homolog distribution. The use of component (d) is of particular advantage with regard to the incorporation of perfumes and the peroxide stability.
Gewerbliche AnwendbarkeitIndustrial applicability
Die erfindungsgemäßen Mittel verleihen wäßrigen Bleichmittel auf Peroxidbasis eine ausreichend hohe und beständige Viskosität. Die Mittel liegen dabei vorzugsweise als wäßrige Zubereitungen vor, die einen nicht-wäßrigen Anteil von 10 bis 50 und vorzugsweise 20 bis 40 Gew.-% aufweisen. Ein weiterer Gegenstand der Erfindung betrifft ihre Verwendung als Verdickungsmittel für wäßrige Wasserstoff¬ peroxidlösungen. Bei den wäßrigen Wasserstoffperoxidlösungen handelt es sich vorzugsweise um wäßrige Bleichmittel des Marktes, die dementsprechend in der Regel einen Aktivsubstanzgehalt von 1 bis 10 und vorzugsweise 5 bis 8 Gew.-% aufweisen. Üblicherweise werden die Mittel in Mengen von 1 bis 5 und vorzugsweise 2 bis 4 Gew.-% - bezogen auf ihren nicht-wäßrigen Anteil und die wäßrigen Wasserstoffperoxidlösungen - eingesetzt. Hilfs- und ZusatzstoffeThe agents according to the invention impart a sufficiently high and stable viscosity to aqueous bleaching agents based on peroxide. The agents are preferably in the form of aqueous preparations which have a non-aqueous content of 10 to 50 and preferably 20 to 40% by weight. Another object of the invention relates to their use as thickeners for aqueous hydrogen peroxide solutions. The aqueous hydrogen peroxide solutions are preferably aqueous bleaches on the market which accordingly generally have an active substance content of 1 to 10 and preferably 5 to 8% by weight. The agents are usually used in amounts of 1 to 5 and preferably 2 to 4% by weight, based on their non-aqueous content and the aqueous hydrogen peroxide solutions. Auxiliaries and additives
Als Hilfs- und Zusatzstoffe können die wäßrigen Wasserstoffperoxidlösungen weitere peroxidstabile Tenside bzw. Hydrotrope enthalten, wie etwa Alkylsulfate, Alkylsulfonate, Alkylbenzolsulfonate, Xylol- sulfonate, Sarkosinate, Tauride, Isethionate, Sulfosuccinate, Ethercarbonsäuren, Betaine, Zuckerester, Aminoxide und Alkyloligoglykoside. Vorzugsweise macht die Summe dieser zusätzlichen Tenside höch¬ stens 10 Gew.-% der Gesamtmenge an Tensiden in der Rezeptur aus. Darüber hinaus können die Mit¬ tel peroxidstabile Duftstoffe, optische Aufheller, Farbstoffe und Pigmente in Mengen von insgesamt 0,01 bis 0,5 Gew.-% - bezogen auf die Mittel - enthalten. Zu den als peroxidbeständig bekannten Duft¬ stoffen zählen beispielsweise monocyclische und bicyclische Monoterpenalkohole sowie deren Ester mit Essig- oder Propionsäure (z.B. Isobomeal, Dihydroterpenöl, Isobornylacetat, Dihydroterpenyl- acetat). Bei den optischen Aufhellern kann es sich beispielsweise um das Kalisalz der 4,4'-bis-(1,2,3- Triazolyl)-(2-)-Stilbin-2,2-sulfonsäure handeln, das unter der Markenbezeichnung Phorwite® BHC 766 vertrieben wird. Als Farbpigmente kommen u.a. grüne Chlorophthalocyanine (Pigmosol® Green, Hostaphine® Green) oder gelbes Solar Yellow BG 300 (Sandoz) in Frage. Die Herstellung der erfin¬ dungsgemäßen Mittel erfolgt mittels Umrühren. Gegebenenfalls kann das erhaltene Produkt zur Abtren¬ nung von Fremdkörpern und/oder Agglomeraten dekantiert oder filtriert werden. The aqueous hydrogen peroxide solutions may contain, as auxiliaries and additives, further peroxide-stable surfactants or hydrotropes, such as, for example, alkyl sulfates, alkyl sulfonates, alkylbenzenesulfonates, xylene sulfonates, sarcosinates, taurides, isethionates, sulfosuccinates, ether carboxylic acids, betaines, sugar esters, amine oxides and alkyl oligoglyides. The sum of these additional surfactants preferably makes up at most 10% by weight of the total amount of surfactants in the formulation. In addition, the agents can contain peroxide-stable fragrances, optical brighteners, dyes and pigments in a total amount of 0.01 to 0.5% by weight, based on the agents. The fragrances known as peroxide-resistant include, for example, monocyclic and bicyclic monoterpene alcohols and their esters with acetic or propionic acid (for example isobomeal, dihydroterpene oil, isobornyl acetate, dihydroterpenyl acetate). The optical brighteners can be, for example, the potassium salt of 4,4'-bis (1,2,3-triazolyl) - (2 -) - stilbin-2,2-sulfonic acid, which is sold under the brand name Phorwite® BHC 766 is distributed. Possible color pigments include green chlorophthalocyanines (Pigmosol® Green, Hostaphine® Green) or yellow Solar Yellow BG 300 (Sandoz). The agents according to the invention are produced by stirring. If necessary, the product obtained can be decanted or filtered to remove foreign bodies and / or agglomerates.
BeispieleExamples
Eine wäßrige Wasserstoffperoxidlösung mit einem Peroxidgehalt von 7 Gew.-% und einem Gehalt von 0,1 Parfümstoff (Isoborneol) wurde mit 3 Gew.-% der erfindungsgemäßen Verdickungsmittel R1 bis R3 der Vergleichsprodukte R4 und R5 in Form 30 Gew.-%iger Lösungen versetzt. Die Viskosität der Lösungen wurde nach der Brookfield-Methode in einem RVT-Viskosimeter (20°C, 10 Upm, Spindel 2) ermittelt. Der Peroxidgehalt sowie das optische Erscheinungsbild wurde nach einer Lagerung von 4 Wochen bestimmt. Die Ergebnisse sind in Tabelle 1 zusammengefaßt (Mengenangaben beziehen sich auf den Aktivsubstanzgehalt und verstehen sich als Gew.-%).An aqueous hydrogen peroxide solution with a peroxide content of 7% by weight and a content of 0.1 perfume (isoborneol) was mixed with 3% by weight of the thickeners R1 to R3 of the comparison products R4 and R5 in the form of 30% by weight solutions transferred. The viscosity of the solutions was determined using the Brookfield method in an RVT viscometer (20 ° C., 10 rpm, spindle 2). The peroxide content and the visual appearance were determined after storage for 4 weeks. The results are summarized in Table 1 (quantitative data relate to the active substance content and are understood as% by weight).
Tabelle 1 Viskosität und LagerstabilitätTable 1 Viscosity and storage stability
*) Crafol® AP-60 * ) Crafol® AP-60

Claims

Patentansprüche claims
1. Verdickungsmittel für wäßrige Wasserstoffperoxidlösungen, enthaltend - bezogen auf den Aktiv- substanzgehalt der Mittel -1. Thickener for aqueous hydrogen peroxide solutions, containing - based on the active substance content of the agent -
(a) 10 bis 90 Gew.-% Fettsäurealkanolamide,(a) 10 to 90% by weight of fatty acid alkanolamides,
(b) 5 bis 20 Gew.-% Alkylethersulfate,(b) 5 to 20% by weight of alkyl ether sulfates,
(c) 0 bis 5 Gew.-% Alkyletherphosphate und(c) 0 to 5% by weight of alkyl ether phosphates and
(d) 0 bis 60 Gew -% Alkylpolyglycolether(d) 0 to 60% by weight alkyl polyglycol ether
mit der Maßgabe, daß sich die Gewichtsangaben zu 100 Gew -% erganzen.with the proviso that the weight details add up to 100% by weight.
2 Mittel nach Anspruch 1 , dadurch gekennzeichnet, daß sie Fettsäurealkanolamide der Formel (I) enthalten,2 compositions according to claim 1, characterized in that they contain fatty acid alkanolamides of the formula (I),
R2 R 2
II.
RiCON(CH2)„OH (I)RiCON (CH 2 ) "OH (I)
in der R1CO für einen aliphatischen, gesättigten oder ungesättigten Acylrest mit 6 bis 22 Kohlenstoff atomen, R2 für Wasserstoff oder einen gegebenenfalls hydroxysubstituierten Alkylrest mit 1 bis 4 Kohlenstoffatomen und n für Zahlen von 2 bis 4 steht.in which R 1 CO represents an aliphatic, saturated or unsaturated acyl radical having 6 to 22 carbon atoms, R 2 represents hydrogen or an optionally hydroxyl-substituted alkyl radical having 1 to 4 carbon atoms and n represents numbers from 2 to 4.
3 Mittel nach den Ansprüchen 1 und 2, dadurch gekennzeichnet, daß sie Alkylethersulfate der Formel (II) enthalten,3 compositions according to claims 1 and 2, characterized in that they contain alkyl ether sulfates of the formula (II),
R30-(CH2CH20)mSθ3X (II)R 3 0- (CH 2 CH 2 0) mSθ3X (II)
in der R3 für einen linearen oder verzweigten Alkyl- und/oder Alkenylrest mit 6 bis 22 Kohlenstoff atomen, n für Zahlen von 1 bis 10 und X für ein Alkali- und/oder Erdalkalimetall, Ammo¬ nium, Alkylammonium, Alkanolammonium oder Glucammonium steht in which R 3 is a linear or branched alkyl and / or alkenyl radical having 6 to 22 carbon atoms, n is a number from 1 to 10 and X is an alkali metal and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium
4. Mittel nach den Ansprüchen 1 bis 3, dadurch gekennzeichnet, daß sie Alkyletherphosphate der Formel (III) enthalten,4. Composition according to claims 1 to 3, characterized in that they contain alkyl ether phosphates of the formula (III),
OXOX
II.
R*(0CH2CH2)P0.P.0R5 (III)R * (0CH 2 CH 2 ) P 0.P.0R5 (III)
in der R4 für einen linearen oder verzweigten Alkylrest mit 6 bis 12 Kohlenstoffatomen, R5 für eine Gruppe R4(OCH2CH2)P oder X, p für Zahlen von 1 bis 5 und X für Wasserstoff, ein Alkali- und/oder Erdalkalimetall steht.in which R 4 is a linear or branched alkyl radical having 6 to 12 carbon atoms, R 5 is a group R 4 (OCH2CH2) P or X, p is a number from 1 to 5 and X is hydrogen, an alkali and / or alkaline earth metal .
5. Mittel nach den Ansprüchen 1 bis 4, dadurch gekennzeichnet, daß sie Alkylpolyglycolether der Formel (IV) enthalten,5. Compositions according to claims 1 to 4, characterized in that they contain alkyl polyglycol ethers of the formula (IV),
R<O(CH2CH20)qH (IV)R <O (CH 2 CH 2 0) q H (IV)
in der R6 für einen Alkyl- und/oder Alkenylrest mit 6 bis 22 Kohlenstoffatomen und q für Zahlen von I bis 10 steht.in which R 6 represents an alkyl and / or alkenyl radical having 6 to 22 carbon atoms and q represents numbers from I to 10.
6. Verwendung von Mitteln nach den Ansprüchen 1 bis 5 als Verdickungsmittel für wäßrige Wasser¬ stoffperoxidlösungen.6. Use of agents according to claims 1 to 5 as thickeners for aqueous hydrogen peroxide solutions.
7. Verwendung nach Anspruch 6, dadurch gekennzeichnet, daß man die Mittel wäßrigen Wasser- stoffperoxidlösungen mit einem Aktivsubstanzgehalt von 1 bis 10 Gew.-% zusetzt.7. Use according to claim 6, characterized in that the agents are added to aqueous hydrogen peroxide solutions with an active substance content of 1 to 10% by weight.
8. Verwendung nach den Ansprüchen 6 und 7, dadurch gekennzeichnet, daß man die Mittel in Mengen von 1 bis 5 Gew.-% - bezogen auf die wäßrigen Wasserstoffperoxidlösungen - einsetzt. 8. Use according to claims 6 and 7, characterized in that the agents are used in amounts of 1 to 5% by weight, based on the aqueous hydrogen peroxide solutions.
EP97927126A 1996-06-13 1997-06-04 Thickening agent for aqueous hydrogen peroxide solutions Expired - Lifetime EP0906404B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19623571A DE19623571C2 (en) 1996-06-13 1996-06-13 Thickener for aqueous hydrogen peroxide solutions
DE19623571 1996-06-13
PCT/EP1997/002890 WO1997047718A2 (en) 1996-06-13 1997-06-04 Thickening agent for aqueous hydrogen peroxide solutions

Publications (2)

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EP0906404A2 true EP0906404A2 (en) 1999-04-07
EP0906404B1 EP0906404B1 (en) 2001-08-16

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WO2004104147A1 (en) * 2003-05-22 2004-12-02 Reckitt Benckiser N.V. Aqueous cleaning compositions

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WO2004067194A2 (en) * 2003-01-31 2004-08-12 Reckitt Benckiser N.V. Aqueous cleaning compositions
WO2004067194A3 (en) * 2003-01-31 2004-11-18 Reckitt Benckiser Nv Aqueous cleaning compositions
AU2004208552B2 (en) * 2003-01-31 2009-05-28 Reckitt Benckiser Vanish B.V. Aqueous cleaning compositions
WO2004104147A1 (en) * 2003-05-22 2004-12-02 Reckitt Benckiser N.V. Aqueous cleaning compositions

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ATE204321T1 (en) 2001-09-15
WO1997047718A2 (en) 1997-12-18
DE19623571A1 (en) 1997-12-18
DE19623571C2 (en) 2000-06-08
WO1997047718A3 (en) 1998-02-12
DE59704318D1 (en) 2001-09-20
EP0906404B1 (en) 2001-08-16
PT906404E (en) 2002-02-28

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